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JCR 2016
جستجوی مقالات
شنبه 6 دی 1404
Iranian Journal of Chemistry and Chemical Engineering
، جلد ۳۹، شماره ۵، صفحات ۳۵-۴۴
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
4-Halo-N-(5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)benzamide and Benzothioamide Derivatives: Synthesis and in vitro Anticancer Assessment
چکیده انگلیسی مقاله
Cancer is a lethal disorder that has caused a serious threat to human health and nowadays there is a crucial need for the development of novel anticancer agents. A new series
of
1,3,4-thiadiazole-based compounds were synthesized and evaluated for anti-cancer properties in vitro.
The synthesis of 5-(Trifluoromethyl)-1,3,4-thiadiazol-2-amine (3) was carried out via solvent-free conditions and consequently, benzamide (4a-4f) and benzothioamide (5a-5f) derivatives bearing halogen moieties (Cl, F) were synthesized. MTT assay was applied for in vitro cytotoxicity assessment against three cancerous cell lines consist of PC3 (Prostate cancer), HT-29 (Colon cancer), and SKNMC (Neuroblastoma). All tested derivatives exhibited equal or more (IC
50
= 3-7 µM) cytotoxic
activity than doxorubicin (IC
50
= 7 µM) as a reference drug against PC3 cell line. Chlorine containing benzamide
as well as benzothioamide derivatives (IC
50
= 14-36
µM) were also exerted a higher cytotoxic activity
against SKNMC cell line compared to
doxorubicin (IC
50
= 40 µM).
کلیدواژههای انگلیسی مقاله
Synthesis,1,3,4-Thiadiazole,Anticancer,MTT assay
نویسندگان مقاله
Ali Reza Aliabadi |
Pharmaceutical Sciences Research Center, Health Institute, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, I.R. IRAN
Hojat Harasami Neek |
Department of Medicinal Chemistry, Faculty of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, I.R. IRAN
Yazdan Bahmani |
Pharmaceutical Sciences Research Center, Health Institute, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, I.R. IRAN
نشانی اینترنتی
https://ijcce.ac.ir/article_38207_873d818b51362e39b3706361c4bdac6e.pdf
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